Coupling System Useful in the Placement of Implants

ABSTRACT

A coupling system is disposed at the distal end of an interventional delivery system for coupling to an implant. The coupling device has a first and second prong connected at one end. The other end of the prongs open or close to release or trap an object, e.g., a bead tethered from an implant. A slot at the distal end of the coupling device allows extra degrees of flexibility for the coupling device.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation application of U.S. application Ser.No. 12/074,272 filed Mar. 3, 2008, now issued as U.S. Pat. No.8,491,627; which is a continuation application of U.S. application Ser.No. 110/389,471 filed Mar. 14, 2003, now issued as U.S. Pat. No.7,344,553; which claims the benefit under 35 USC §119(e) to U.S.application Ser. No. 60/382,528 filed May 21, 2002 and to U.S.Application Ser. No. 60/364,017 filed Mar. 15, 2002, both now expired.The disclosure of each of the prior applications is considered part ofand is incorporated by reference in the disclosure of this application.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The invention generally involves coupling or attaching devices used in atranscatheter delivery system and their uses in connection withdelivering or retrieving a medical implant.

2. Background Information

Numerous systems for percutaneous transcatheter delivery of implantshave been devised over the years in order to assist physicians indelivering and positioning implants, for example, occluders, within apatient, preferably in a minimally invasive manner. A problem with manyof the known delivery systems is that they can often adversely affectpositioning of the device that is being implanted, which forces thedoctor to estimate and take into consideration such effect whenassessing the final implant position prior to releasing the implant.

For example, most of the delivery systems include an elongated catheterthat is used to access various passageways inside a patient's body.Often the desired position of the implant may not align with thelongitudinal axis of the catheter. If the juncture between the implantand the catheter lacks sufficient flexibility, tension and torque willbe generated at the juncture when the implant has to be bent off thecatheter's axis in order to assume the desired position. Upon release ofthe implant, the tension and torque will affect both the implant and thedelivery catheter, causing shifting in the implant position, andpossible trauma to the surrounding tissue as the distal end of thecatheter springs back to a more relaxed state. Such shifting in theimplant position may result in a less desirable medical result (such asdevice embolization or a residual leak in the case of septal occluders).

Implants may include devices designed for compression into a small sizetube or catheter to facilitate their introduction into the vasculatureof the patient. The implants are subsequently expandable either toocclude defects or holes in the heart, in the case of septal occluders,or to contact the walls of the passageway (e.g., blood vessels), in thecase of vena cava filters or stents. Among these devices are septaloccluders well-known in the art such as the occluder described in U.S.Pat. No. 5,425,744 issued to Fagan et al. Septal occluders are useful intreating medical conditions such as patent foramen ovale (PFO), which isa persistent, one-way, often flap-like opening in the wall between theright atrium and left atrium of the heart, as well as other congenitaland acquired defects in the heart or vasculature.

Presently, ball-to-ball (or pin-to-pin) attach/release mechanisms, suchas the attach/release mechanism illustrated in Transcatheter Therapy inPediatric Cardiology (1993): 335-348, have been employed by one skilledin the art to implant and position such septal occluders within theheart. The pin-to-pin mechanism illustrates the adverse effect theattachment juncture may cause in the positioning of the implant. Withpin-to-pin mechanisms, the implant, a septal occluder, for example, isheld nearly perpendicular to the longitudinal axis of a sleeve on thedistal end of the delivery catheter. Due to the acute angle of deliveryof the septal occluder from the inferior vena cava to the septal wall,the rigid pin-to-pin connection applies tension to the implant and theunderlying septum, and compromises precise assessment of the finalimplant position prior to release of the implant.

Other types of attachment mechanisms known in the art include threadedmale and female members as described in U.S. Pat. No. 5,725,552 issuedto Kotula et al. This system, however, requires axial rotation of themembers with respect to each other to disconnect the delivery device andalso provides little flexibility, if any, for the lateral pivoting ofthe implant at the point it is attached to the delivery device.

Accordingly, there is a need for an interventional delivery system thatallows assessment of proper positioning of an implant prior to releaseby the catheter.

SUMMARY OF THE INVENTION

The present invention provides novel and improved coupling systems andrelated methods, which may be useful for delivering, repositioning, andremoval of an implant, such as a septal occluder, into and out of apatient.

The invention relates to a coupling device that allows pivoting of theimplant at or near the juncture where the implant couples with thedistal end of a delivery catheter, which is the coupling device.Specifically, the juncture is designed with a slot, for example, in theshape of a half-circle arc, that allows implant pivoting in a planealong the longitudinal axis of the coupling device. That feature, plus atrapping mechanism that allows implant rotation about the longitudinalaxis of the coupling device, provides the much needed flexibility toavoid generating the tension that would otherwise cause bending at thecoupling juncture and resulting in distortion of the underlying septum.Accordingly, after being released, the implant will stay where it wasintended and the newly freed distal end of the delivery system will haveless tendency to spring back and cause trauma to the surrounding tissue.

According to one aspect of the invention, a coupling or attachmentdevice with a distal end is provided. The coupling device has anassembly that includes at least two prongs. Each of the prongs has afirst and a second end. The prongs are connected at their first ends andfree at their second ends. The second end of at least one of the prongsis movable from two positions: in an open position, the second ends ofthe two prongs are apart from each other; in a closed position, thesecond ends of the prongs are closer to each other than in the openposition. Also in the closed position, the second ends of the two prongsdefine a slot at the distal end of the coupling device. The slot may beused for coupling an object to the coupling device, and is part of thesolution to provide more flexibility at the coupling juncture. In oneembodiment, the slot is an arc that spans about 180 degrees.

According to another aspect, the second end of only one prong ismoveable. The other prong is fixed relative to the longitudinal axis ofthe coupling device.

According to yet another aspect of the invention, either the couplingdevice or the implant contains at least a portion that is magnetic. Inone embodiment, at least a portion of at least one of the prongs ismagnetic.

In one embodiment of the invention, at least one of the prongs isspring-biased. In one embodiment, the coupling device further includes asleeve that moves relative to the prongs. The sleeve forces the prongstowards the closed position when the sleeve slides over at least aportion of the prongs. The prongs open into the open position whenextended from the sleeve.

In another embodiment, at least one of the prongs has a recess, cavity,socket, concavity, cup, dent, or hole for receiving and trapping atleast an object, such as a portion of an implant. The cavity may conformto the shape of the object such that when the object is trapped insidethe cavity, the object is able to rotate about its own axis.

According to yet another aspect of the invention, the coupling device ofthe invention is assembled into an interventional delivery system thatdelivers an implant into a patient. The delivery system has a tubularportion with a lumen, and a core wire that slides inside the lumen ofthe tubular portion. The coupling device is disposed at the distal endof the core wire and is coupled to an implant.

In one embodiment, the implant has a tip that is spherical, and it fitsa spherical cavity in the coupling device when the prongs of thecoupling device are at the closed position. In one embodiment, theimplant is a septal occluder. In another embodiment the implant is anatrial appendage occlusion device or prosthesis.

A method for coupling an object is also provided herein to practice theinvention. A coupling device according to the invention is provided. Anobject is coupled to the device when at least a tip of the object istrapped inside a cavity in the coupling device. The object may beallowed to pivot in the slot at the distal end of the coupling device.

BRIEF DESCRIPTION OF THE DRAWINGS

In the drawings, like reference numbers generally refer to the sameparts throughout the different views. Also, the drawings are notnecessarily to scale, emphasis instead generally being placed uponillustrating the principles of the invention.

FIG. 1 is a plan view of an embodiment of an interventional deliverysystem with an implant linked to a coupling device disposed at thedistal end of the interventional delivery system.

FIG. 2A is a perspective view of the distal end of an interventionaldelivery system including a coupling device in an open position inaccordance with an embodiment of the present invention.

FIG. 2B illustrates a longitudinal cross-section of the embodiment ofthe distal end of an interventional delivery system illustrated in FIG.2A.

FIGS. 2C and 2D illustrate the embodiment shown in FIGS. 2A and 2Btransition into a closed position to capture an implant

FIG. 3A is a perspective view of a portion of another embodiment of acoupling device according to the invention.

FIG. 3B is a partial cross-sectional view of an embodiment of a couplingdevice according to the invention.

FIG. 3C is a partial cross-sectional view of the embodiment of FIG. 3Brotated 90° and with part of an implant trapped therein.

FIG. 3D is a partial cross-sectional view of the embodiment of FIG. 3Bdevice with part of an implant trapped therein.

FIG. 3E is a partial cross-sectional view of the embodiment of FIG. 3Bin an open position.

FIGS. 4A-4C are perspective views at various angles of an embodimentaccording to the invention.

FIG. 4D is a perspective view of a portion of the embodiment shown inFIGS. 4A-4C.

DETAILED DESCRIPTION OF THE INVENTION

An interventional delivery system described herein includes a tubularportion, a core wire that slides in the lumen of the tubular portion,and a coupling device at the distal end of the core wire that couples toan implant

Referring to FIG. 1, in accordance with the present invention, acoupling device 1 disposed at the distal end 5 of an interventionaldelivery system 2 provides a mechanism for pivoting an implant 3 (e.g.,a septal occluder) with respect to the coupling device 1 in order toavoid bending or twisting of the distal end 5 of the delivery system 2during the delivery of the implant 3. In one embodiment according to theinvention, the interventional delivery system 2 may include a distalsleeve 4 connected to a tubular body portion 6, which can be a catheterhaving a proximal end 11 connected to a handle 8. As an example, theimplant 3 is shown to be a septal occluder planted in an opening in theatrial septum 9.

The term “implant” used herein includes devices, carriers, and objectsthat are placed in the body of a patient by invasive or minimallyinvasive methods, including but not limited to, prosthetic occluders,stents, filters, prostheses, valves, pumps, pace-makers, medications andso on. The implant may be permanent, semi-permanent, or temporary. Theimplant may be biodegradable. The implant may be removable through aninterventional procedure. The implant may be a drug delivery device,such as capsules, tablets, or suppositories, for example, those thatdeliver pharmaceutical agents to the patient. In particular, the termimplant includes intracardiac prosthetic occluders, for example, aseptal occluder for the closing of, for example, patent foramen ovale,and an atrial appendage occlusion device or prosthesis.

With reference to FIGS. 2A-2D, in one embodiment according to theinvention, the distal end 5 of the interventional delivery system 2includes a distal sleeve 4. Inside the lumen 10 of the distal sleeve 4,a core wire 12 is able to slide relative to the distal sleeve 4. Thesliding of the core wire 12 can be controlled through the handle 8 (FIG.1). A coupling/gripping device 1 is secured to the distal end 14 of thecore wire 12. There are a variety of ways to secure the coupling device1 to the core wire 12, e.g., by extrusion, welding, soldering, molding,threading or by an adhesive. Being secured to core wire 12 enables thecoupling device 1 and the distal sleeve 4 to move relative to oneanother. The sleeve 4 may be further enclosed in a catheter.

The coupling device 1 includes an assembly of two or more prongs. Inthis embodiment, two gripping prongs 15 and 15′, each resembling alobster claw, are positioned opposite each other. Prongs 15 and 15′ eachhas a distal end 16, 16′ respectively, and a proximal end 17, 17′respectively.

The prongs 15 and 15′ are connected like pincers by a pin or pivot 18,at their proximal ends 17, 17′, and are free, i.e., not connected at thedistal ends 16, 16′. As a result, when the distal ends 16 and 16′ areapart, the coupling device 1 is at an open position (e.g., FIG. 2A). Incontrast, when the distal ends 16 and 16′ are closer to each other, thecoupling device 1 is at a closed position (e.g., FIG. 2D). In oneembodiment of the invention, both prongs 15 and 15′ pivot or turn aboutthe pivot 18. In the embodiment shown in FIGS. 2A-2D, however, only oneprong 15 is movable; the other prong 15′ is fixed to the distal end 14of the core wire 12 and does not pivot or articulate relative to thelongitudinal axis of the core wire 12. Making only one prong moveable orpivotable relative to the core wire 12 decreases the cost of manufactureand lengthens the life span of the coupling device 1 because chances formechanical misalignment are substantially reduced when the prongs 15,15′ close upon being retracted into the distal sleeve 4.

Referring to FIGS. 2B-2D, a spring member 20, e.g., a V-shaped wire, isdisposed between the prongs 15 and 15′, and biased to force the prong 15outward towards the open position. The spring member 20 may beintegrated into at least one of the prongs or may remain as a separatecomponent. The spring member 20 can be manufactured from any suitablematerials, e.g., stainless steel or nitinol.

Referring now to FIGS. 2A and 2B, the distal sleeve 4 is sized andshaped to slide over or enclose the prongs 15, 15′. When the prongs 15,15′ are extended entirely outside the distal sleeve 4, the couplingdevice 1 is in the open position (FIG. 2B). The distal end 16 of thefirst prong 15 is apart from the distal end 16′ of the second prong 15′such that an intended target object is not secured by the couplingdevice 1. The target object can be of a variety of shapes, such ascubes, cylinders, cones, spheres, and so on. One embodiment of a targetobject is a spherical bead 22 linked to a main body 23 of the implant 3through a tether 25. The tether 25 may be a wire, a thread, a strut, atie with no particular limitation on its flexibility.

Referring now to FIG. 3 A, at least one of the prongs, for example,prong 15 of the coupling device 1 has a cavity 27 to grip and trap thetarget object. Further, there may be cavities 27, 27′ in the distal ends16, 16′ of both the prongs 15 and 15′ as shown, for example, in FIG. 2B.Cavities 27, 27′ are preferably shaped to conform to the shape of thetarget object, e.g., the bead 22 of the implant 3. In other words, bothcavities 27 and 27′ are substantially a half-spherical concavity andtogether form a spherical concavity. Referring now to FIG. 2D, cavities27, 27′ may also be sized to allow the implant 3 to rotate about thetether 25 as shown by arrows “A” when the prongs 15 and 15′ are in theclosed position.

Referring to FIGS. 2B, 2C and 3A, each of the prongs 15 and 15′ may alsoinclude recesses 30 and 30′ adjacent the cavities 27 and 27′respectively. Referring to FIG. 3B, the recesses 30 and 30′ togetherfowl a slot 33 between the prongs 15 and 15′ when the prongs 15 and 15′are in the closed position. The slot 33 may be an arc spanning between 0to 360°, e.g., about 90° or 270°, or 180° as illustrated in FIGS. 3A and3B. Referring to FIGS. 2D, 3C, and 3D, the slot 33 is sized to fit thetether 25 that links the trapped bead 22 to the main body 23 of theimplant 3. Referring again to FIG. 1, when the prongs 15 and 15′ are inthe closed position and the bead 22 is trapped by the cavities 27 and27′, the tether 25′may pivot in the slot 33 in an arc indicated byarrows “B,” providing the implant 3 with the crucial ability to pivot atthe coupling juncture without causing undesired tension to the distalend 5 of the interventional delivery system 2. The slot 33 and thecavities 27, 27′, which provide axial rotation for the implant 3,together enable a medical personnel to position the implant 3 in avariety of orientations without having to bend the delivery catheter.

Referring back to FIG. 2D, in one embodiment according to the invention,the distal ends 16, 16′ of the prongs 15 and 15′, may have a largerouter diameter than the proximal ends 17, 17′, creating a cap 35 or amushroom head. In the closed position illustrated, e.g., in FIG. 2D, theouter diameter of the combined distal ends 16, 16′, is larger than thelumenal diameter 31 of the distal sleeve 4. And the lumenal diameter 31of the distal sleeve 4 is larger than the outer diameter 34 of theproximal ends 17, 17′ combined and measured at the closed position. As aresult, the distal sleeve 4 is slideably moveable over the proximal ends17, 17′ as shown in FIG. 2C, but the distal rim 19 of the distal sleeve4 will stop when the rim 19 abuts the cap 35, as shown in FIG. 2D. Themushroom head shape sets a limit to the relative positions between thedistal sleeve 4 and the coupling device 1, and can assist an operator indetermining the precise length of sliding required of the distal sleeve4 to release the captured implant 3.

Referring again to FIGS. 2A-2D, when the distal sleeve 4 moves distallytowards the coupling device 1, the distal rim 19 of the distal sleeve 4hits the moveable prong 15, and starts to force the prong 15 to movefrom the open position illustrated in FIG. 2A to the closed positionillustrated in FIG. 2D. The space between the cavities 27 and 27′ alsostarts to decrease. FIG. 2C illustrates the “pivot point” 38 on themoveable prong 15. A pivot point is the point on the outer wall of theprongs 15, 15′ that, when the distal rim 19 of the distal sleeve 4advances to it, the space between the cavities 27 and 27′ has decreasedsuch that the bead 22, if captured, can no longer exit the cavities 27and 27′. Referring to FIGS. 2C and 2D, when the distal rim 19 of thedistal sleeve 4 is positioned between the pivot point 38 on the proximalportion 17 and the cap 35, the implant is reversibly secured or coupledto the coupling device 1. The distance between the pivot point 38 andthe cap 35 where the distal sleeve 4 cannot advance any further, iscalled the “float range” 40.

In a particular embodiment, the “float range” 40 is maximized, e.g., tosubstantially equal the entire length of the proximal ends 17, 17′ bypositioning the pivot point 38 as proximal on the proximal ends 17, 17′as possible. Referring to FIG. 2D, this may be achieved by minimizingthe clearance between the inner wall of the distal sleeve 4 and theouter wall of the proximal ends 17, 17′ of the coupling device 1 whenthe device 1 is in the closed position. In other words, there can beprovided a distal sleeve 4 whose lumenal diameter 31 is as close aspossible to the outer diameter 34 of the proximal ends 17, 17′ of thecoupling device 1 at the closed position. In a particular embodiment,the lumenal diameter 31 and the outer diameter 34 are substantially thesame. As long as the distal rim 19 of the distal sleeve 4 is within the“float range” 40, the bead 22 of the implant 3 will be trapped insidethe cavities 27 and 27′ of the coupling device 1, minimizing inadvertentrelease of the implant 3.

The material for the prongs 15, 15′ may include but is not limited tostainless steel, titanium, nitinol, etc. One embodiment of the inventiontakes advantage of the elasticity in the material, such as nitinol, usedfor the prongs 15, 15′. Referring to FIG. 3A, at least one of theprongs, e.g., the prong 15, may include a portion 42 that is reduced inwidth for extra flexibility between the distal end 16 and the proximalend 17. Referring to 3E, because the elasticity in the material for theprongs 15, 15′, the distal ends 16, 16′ will bend or pivot with respectto the proximal ends 17, 17′ respectively. Accordingly, when the distalends 16, 16′ are outside the distal sleeve 4, the distal ends 16, 16′will bend away from each other into the open position. In thisembodiment, there is no need for a spring member in between the prongs15, 15′ in order to achieve the open position.

In the exemplary embodiment shown in FIGS. 2A-2D, one of the prongs 15′is longer than the other prong 15, and the proximal end 17′ of the prong15′ is fixedly secured to the distal end of the core wire 12. Theproximal end 17 of the other prong 15 is pivotally joined, by a pin 18,to the proximal end 17′ of the longer prong 15′. Therefore, the openingand closing of the coupling device 1, in this embodiment, depends on themovement of the prong 15. In another embodiment shown in FIGS. 4A-4C,the proximal end 17′ of the prong 15′ is not fixedly secured to the corewire 12, but pinned together with a distal end 45 of a connector piece43 and the proximal end 17 of the prong 15, all through the pin 18. Theproximal end 46 of the connector piece 43 is, in turn, connected to thedistal end 14 of the core wire 12 through, e.g., a ball-and-socket joint44. A more detailed view of one of the prongs, e.g., the prong 15′, isprovided in FIG. 4D.

Referring back to FIG. 2A, in another aspect of the invention, eitherthe coupling device 1 or the implant 3 contains at least a portion thatis magnetic. For example, the prongs 15 and 15′ can be magnetic, and theimplant bead 22 may be ferromagnetic. Such magnetic properties make iteasier to capture or recapture the bead 22, which can be very small.

The present system contemplates a coupling system between the catheterand implant, such as a septal occluder, which provides pivoting andaxial rotation in order to minimize forces exerted on the device as wellas the septum of the heart. The system may have more than two prongs inaccordance with the invention. For example, a system with four prongsmay have two slots forming a cross-like section that allows the trappedimplant tip to move in two orthogonal planes defined by the slots.

The present invention also includes methods related to the systemsdescribed above including methods of using the system. Referring back toFIG. 1, once the prongs of the coupling device 1 have trapped part ofthe implant 3, and the coupling device 1 has been at least partiallyretracted into the distal sleeve 4, the doctor can extend theinterventional delivery system 2 with its distal end 5 coupled to theimplant 3 into a body lumen such as the vascular passageway. Once thedistal end 5 of the delivery system 2 reaches the target region, e.g.,an opening in the atrial septum 9, the implant 3, e.g., a septaloccluder, may be rotated about the axis of the core wire 12 of thedelivery system 2. Moreover, the doctor may pivot the implant 3 by itstether 25 with respect to the coupling device 1 along the slot 33 formedbetween the prongs of the coupling device 1 as indicated by the arrow“B”. The rotation and pivoting action minimize forces acting on thecoupling device 1 and the atrial septum 9 where the implant 3 isimplanted.

Once the implant 3 is satisfactorily positioned within the cardiacchamber, the doctor may release the implant 3, e.g., by pushing anactuating button 7 on the handle 8 to advance the core wire 12 and thecoupling device 1 out of the distal sleeve 4 into the open position.Conversely, when retrieving or repositioning the implant 3, the couplingdevice 1 would be actuated to the open positioned to capture the implant3, e.g., by its tethered bead. Then, the coupling device 1 is at leastpartially retracted into the distal sleeve 4, forcing the prongs tocollapse into the closed position and trapping the bead of the implant3. As described above, magnetism in either or both the coupling device 1and the implant 3 would aid the recapturing of the implant 3. After theimplant 3 has been recaptured by the coupling device 1, the doctor maymaneuver the interventional delivery system 2 to a desired location toreposition the implant 3 or out of the patient's body to remove theimplant 3.

Other Embodiments

The invention may be embodied in other specific forms without departingfrom the spirit or essential characteristics thereof. The presentembodiments are therefore to be considered in all respects asillustrative and not restrictive, the scope of the invention beingindicated by the appended claims rather than by the foregoingdescription, and all changes which come within the meaning and range ofequivalency of the claims are therefore intended to be embraced therein.

What is claimed is:
 1. A device for coupling an implant, the devicecomprising: a distal end; a pivot; a first prong and a second prong eachcomprising a first end and a second end, the first prong and secondprong being connected by the pivot at their first ends and free at theirsecond ends, each of said first and second prongs having an outersurface and an inner surface, the inner surface of at least one of theprongs comprising a recess, the inner surface of the second end of eachprong comprising a cavity, the proximal end of the cavity terminatingdistal to the pivot, at least one of the first prong and the secondprong being reversibly movable between an open position and a closedposition; and the at least one recess forming a slot comprising aproximal end, a distal end, the proximal end of the slot terminatingdistal to the pivot, the slot being defined by the second end of atleast one of the prongs when the first prong and the second prong are inthe closed position.
 2. The device of claim 1, further comprising asleeve slideably moveable relative to the first and second prongs, thesleeve forcing the second end of at least one of the prongs toward theclosed position when the sleeve slides over at least a portion of theprongs.
 3. The device of claim 1, wherein the cavity is shaped toconform to the shape of the implant wherein the implant is capable ofrotating within the cavity.
 4. The device of claim 1, further comprisinga sleeve slideably moveable relative to the prongs, the sleeve defininga lumen, wherein the prongs are in the closed position when the firstends of the prongs are enclosed in the lumen of the sleeve and theprongs are in the open position when the first ends of the prongs extendout of the lumen of the sleeve.
 5. The device of claim 1, furthercomprising a sleeve comprising an outer diameter, wherein the outerdiameter of the sleeve is smaller than the outer diameter of the secondend of the first prong and the second end of the second prong when thefirst prong and the second prong are together in the closed position. 6.An interventional delivery system for delivering an implant into apatient, comprising: a tubular portion defining a lumen; a core wirecomprising a distal end and having a longitudinal axis, the core wireslideably moveable in the lumen of the tubular portion; and a couplingdevice at the distal end of the core wire, the coupling devicecomprising a distal end, a pivot, a first prong and a second prong eachcomprising a first end and a second end, the first prong and secondprong being connected by the pivot at their first ends and free at theirsecond ends, each of said first and second prongs having an outersurface and an inner surface, the inner surface of at least one of theprongs comprising a recess, the inner surface of the second end of eachprong comprising a cavity, the proximal end of the cavity terminatingdistal to the pivot, and at least one of the first prong and the secondprong being reversibly movable between an open position and a closedposition, and the at least one recess forming a slot comprising aproximal end, a distal end, the proximal end of the slot terminatingdistal to the pivot, the slot being defined by the second end of atleast one of the prongs when the first prong and the second prong are inthe closed position.
 7. The system of claim 6, further comprising ahandle connected to the tubular portion, the handle comprising anactuator for actuating the core wire.
 8. The system of claim 6, furthercomprising a sleeve slideably moveable relative to the first and secondprongs, the sleeve forcing the second end of at least one of the prongstoward the closed position when the sleeve slides over at least aportion of the prong.
 9. The system of claim 6, further comprising animplant.
 10. The system of claim 9, wherein the implant comprises a tipand the cavity in each prong is shaped to conform to the shape of theimplant tip wherein the implant tip is capable of rotating within thecavity.
 11. The system of claim 9, wherein the implant comprises aseptal occluder.
 12. The system of claim 9, wherein the implantcomprises an atrial appendage occlusion device.
 13. The system of claim6, further comprising a sleeve comprising an outer diameter, wherein theouter diameter of the sleeve is smaller than the outer diameter of thesecond end of the first prong and the second end of the second prongwhen the first prong and the second prong are together in the closedposition.
 14. A method for coupling an implant, the method comprising:providing a coupling device comprising a distal end, a pivot, a firstprong and a second prong each comprising a first end and a second end,the first prong and second prong being connected by the pivot at theirfirst ends and free at their second ends, each of said first and secondprongs having an outer surface and an inner surface, the inner surfaceof at least one of the prongs comprising a recess, the inner surface ofthe second end of each prong comprising a cavity, the proximal end ofthe cavity terminating distal to the pivot, at least one of the firstprong and the second prong being reversibly movable between an openposition, and a closed position, and a slot comprising a proximal end, adistal end, and an arc shape extending from the distal end of thedevice, the slot being defined by the second end of at least one of theprongs when the first prong and the second prong are in the closedposition; and trapping at least a tip of an implant in the cavity in atleast one of the prongs.